WO2004013227A1 - Matiere moulable ininflammable - Google Patents

Matiere moulable ininflammable Download PDF

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Publication number
WO2004013227A1
WO2004013227A1 PCT/EP2003/007681 EP0307681W WO2004013227A1 WO 2004013227 A1 WO2004013227 A1 WO 2004013227A1 EP 0307681 W EP0307681 W EP 0307681W WO 2004013227 A1 WO2004013227 A1 WO 2004013227A1
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Prior art keywords
weight
composition according
parts
graft
component
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PCT/EP2003/007681
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German (de)
English (en)
Inventor
Andreas Seidel
Thomas Eckel
Dieter Wittmann
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Bayer Materialscience Ag
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Application filed by Bayer Materialscience Ag filed Critical Bayer Materialscience Ag
Priority to JP2004525205A priority Critical patent/JP2005534755A/ja
Priority to MXPA05001112A priority patent/MXPA05001112A/es
Priority to CA002494349A priority patent/CA2494349A1/fr
Priority to BR0305682-1A priority patent/BR0305682A/pt
Priority to AU2003254360A priority patent/AU2003254360A1/en
Priority to EP03766177A priority patent/EP1527136A1/fr
Publication of WO2004013227A1 publication Critical patent/WO2004013227A1/fr

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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/49—Phosphorus-containing compounds
    • C08K5/51—Phosphorus bound to oxygen
    • C08K5/52—Phosphorus bound to oxygen only
    • C08K5/521—Esters of phosphoric acids, e.g. of H3PO4
    • C08K5/523—Esters of phosphoric acids, e.g. of H3PO4 with hydroxyaryl compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L69/00—Compositions of polycarbonates; Compositions of derivatives of polycarbonates
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/49—Phosphorus-containing compounds
    • C08K5/51—Phosphorus bound to oxygen
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • C08L51/04—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to rubbers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
    • C08L67/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds

Definitions

  • the present invention relates to flame-retardant polycarbonate molding compositions with an enlarged working window, containing graft polymer, polyalkylene terephthalate and oligomeric phosphoric acid esters based on bisphenol A.
  • Molding compositions in particular have a high weld line strength, but show an increased tendency to form stress cracks under the action of chemicals at higher processing temperatures.
  • EP-A 0 363 608 describes polymer mixtures composed of aromatic polycarbonate, styrene-containing copolymer and / or graft copolymer and oligomeric phosphates and fluorinated polyolefins as flame retardant additives.
  • aromatic polycarbonate styrene-containing copolymer and / or graft copolymer
  • oligomeric phosphates and fluorinated polyolefins as flame retardant additives.
  • EP-A 0 594 021 describes polymer mixtures of aromatic polycarbonate, polyalkylene terephthalate, graft polymer and resorcinol-bridged oligomeric phosphoric acid esters and fluorinated polyolefins as flame retardant additives. Molded parts made from these molding compounds, which were manufactured at low processing temperatures, have a high resistance to stress cracking. Shaped articles made from these mixtures also have high impact strength and surface quality. At higher processing temperatures, as are often necessary for the production of thin-walled parts in particular, experience has shown that such molding compounds often show stress cracking problems.
  • the object of the present invention is to provide flame-retardant compositions with good heat resistance, which can be processed at high processing temperatures of up to 300 ° C. into thin-walled moldings with improved mechanical properties, in particular increased resistance to stress cracking failure under the influence of chemicals, and in addition are characterized by a combination of high weld line strength and elongation at break.
  • polycarbonate / ABS compositions have the desired profile of properties which contain polyalkylene terephthalate and, as a flame retardant additive, an oligomeric phosphoric acid ester based on bisphenol A. These molding compositions are particularly suitable for producing thin-walled materials
  • molded parts made from the compositions according to the invention show excellent resistance to stress cracking failure under the influence of chemicals.
  • the molding compounds have significantly improved bond seam strengths compared to flame-retardant PC / AB S molding compounds with comparable processing characteristics (i.e. melt flowability).
  • the invention relates to flame-retardant, thermoplastic molding compositions
  • R1, R2, R3, R4 independently of one another Ci-Cg-alkyl, Cs-Cg-cycloalkyl, C 6 -C 10 aryl or C 7 -C 12 aralkyl,
  • n independently of one another 0 or 1, preferably 1,
  • R 5 and R 6 independently of one another Ci -C 4 alkyl, especially methyl m independently of one another 0, 1, 2, 3 or 4 and
  • composition according to the invention contains polycarbonate and / or polyester carbonate, preferably aromatic polycarbonate and / or polyester carbonate.
  • Aromatic polycarbonates and / or aromatic polyester carbonates according to component A which are suitable according to the invention are known from the literature or can be prepared by processes known from the literature, such as phase boundary or melt polymerization processes (for the production of aromatic polycarbonates, see for example Schnell, "Chemistry and Physics of Polycarbonates", Interscience Publishers, 1964 and
  • Aromatic polycarbonates are produced e.g. by implementing
  • Diphenols with carbonic acid halides preferably phosgene and / or with aromatic Matic dicarboxylic acid dihalides, preferably benzenedicarboxylic acid dihalogenides, by the interfacial process, optionally using chain terminators, for example monophenols and optionally using trifunctional or more than functional branching agents, for example triphenols or tetraphenols.
  • Diphenols for the preparation of the aromatic polycarbonates and or aromatic polyester carbonates are preferably those of the formula (II)
  • A is a single bond, C. to C. alkylene, C. to C. alkylidene, C. to C fi -cycloalkylidene, -O-, -SO-, -CO-, -S-, -SO 2 - , C. to C_ 2 -arylene, to which further aromatic rings optionally containing heteroatoms may be condensed,
  • R 5 and R 6 can be selected individually for each X 1 , independently of one another hydrogen or C. to C, alkyl, preferably hydrogen, methyl or ethyl,
  • n is an integer from 4 to 7, preferably 4 or 5, with the proviso that at least one atom X 1 , R 5 and R 6 are simultaneously alkyl.
  • Preferred diphenols are hydroquinone, resorcinol, dihydroxydiphenols, bis- (hydroxy ⁇ henyl) -C.-C.-alkanes, bis- (hydroxyphenyl) -C 5 -C 6 -cycloalkanes, bis- (hydroxyphenyl) ether, bis- ( hydroxyphenyl) sulfoxides, bis (hydroxyphenyl) ketones, bis (hydroxyphenyl) sulfones and ⁇ , ⁇ -bis (hydroxyphenyl) diisopropyl benzenes.
  • diphenols are 4,4'-dihydroxydiphenyl, bisphenol-A, 2,4-bis (4-hydroxy ⁇ henyl) -2-methylbutane, 1,1-bis (4-hydroxyphenyl) cyclohexane, 1,1-bis- (4-hyckoxyphenyl) -3.3.5-trimethylcyclohexane, 4,4'-dihydroxydiphenyl sulfide and 4,4'-dihydroxydiphenyl sulfone.
  • 2,2-Bis- (4-hydroxyphenyl) propane (bisphenol-A) is particularly preferred.
  • the diphenols can be used individually or as any mixtures.
  • the diphenols are known from the literature or can be obtained by processes known from the literature.
  • thermoplastic, aromatic polycarbonates Suitable for the production of thermoplastic, aromatic polycarbonates
  • Chain terminators are, for example, phenol, p-tert-butylphenol but also long-chain alkylphenols, such as 4- (1,3-tetramethylbutyl) phenol according to DE-A 2 842 005 or monoalkylphenol or dialkylphenols with a total of 8 to 20 colile atoms in the alkyl substituents such as 3,5-di-tert-butylphenol, p-iso-octylphenol, p-tert-octylphenol, p-dodecylphenol and 2- (3,5-dimethylheptyl) phenol and 4- (3,5-di- methylheptyl) phenol.
  • the amount of chain terminators to be used is generally between 0.5 mol% and 10 mol%, based on the molar sum of the diphenols used in each case.
  • thermoplastic, aromatic poly (ester) carbonates have average weight-average molecular weights (M w , measured, for example, by means of an ultracentrifuge, scattered light measurement or gel permeation chromatography) from 10,000 to 200,000, preferably 15,000 to 80,000, particularly preferably 17,000 to 40,000, in particular 18,000 up to 35,000.
  • M w average weight-average molecular weights
  • thermoplastic, aromatic polycarbonates can be branched in a known manner, preferably by incorporating 0.05 to 2.0 mol%, based on the sum of the diphenols used, of three-functional or more than three-functional compounds, for example those with three and more phenolic see groups.
  • copolycarbonates Both homopolycarbonates and copolycarbonates are suitable.
  • copolycarbonates according to component A according to the invention 1 to 25% by weight, preferably 2.5 to 25% by weight, based on the total amount of diphenols to be used, polydiorganosiloxanes with hydroxyaryloxy end groups can also be used. These are known (US 3,419,634) and are known from the literature Process can be produced. The production of polydiorganosiloxane-containing copolycarbonates is described in DE-A 3 334 782.
  • preferred polycarbonates are the copolycarbonates of bisphenol A with up to 15 mol%, based on the molar sum of diphenols, of other diphenols mentioned as preferred or particularly preferred.
  • Aromatic dicarboxylic acid dihalides for the production of aromatic polyester carbonates are preferably the diacid dichlorides of isophthalic acid, terephthalic acid, diphenyl ether-4,4'-dicarboxylic acid and naphthalene-2,6-dicarboxylic acid.
  • a carbonic acid halide preferably phosgene, is additionally used as the bifunctional acid derivative.
  • the amount of chain terminators is in each case 0.1 to 10 mol%, based on mol of diphenol in the case of the phenolic chain terminators and on mol of dicarboxylic acid dichlorides in the case of monocarboxylic acid chloride chain terminators.
  • the aromatic polyester carbonates can also contain built-in aromatic hydroxycarboxylic acids.
  • the aromatic polyester carbonates can be linear or branched in a known manner (see DE-A 2 940 024 and DE-A 3 007 934).
  • branching agents which can be used are branched or melamine-functional carboxylic acid chlorides, such as trimesic acid trichloride, cyanuric acid trichloride, 3,3 '-, 4,4'-benzophenonetetracarboxylic acid tetrachloride, 1,4,5,8-naphthalenetetracarboxylic acid tetrachloride or pyromellitic acid tetrachloride .01 to 1.0 mol% (based on the dicarboxylic acid dichlorides used) or trifunctional or multifunctional phenols, such as phloroglucin, 4,6-dimethyl-2,4,6-tri- (4-hydroxyphenyl) -hepten-2 '' , 4,6-Dimethyl-2,4- 6-tri- (4-hydroxyphenyl) heptane, l, 3,5-tri- (4-hydroxyphenyl) benzene, l, l, l-tri- (4- hydroxy
  • the proportion of carbonate structural units in the thermoplastic, aromatic polyester carbonates can vary as desired.
  • the proportion of carbonate groups is preferably up to 100 mol%, in particular up to 80 mol%, particularly preferably up to 50 mol%, based on the sum of ester groups and carbonate groups.
  • Both the ester and the carbonate content of the aromatic polyester carbonates can be present in the form of blocks or randomly distributed in the polycondensate.
  • thermoplastic, aromatic polycarbonates and polyester carbonates can be used alone or in any mixture.
  • Component B is
  • the polyalkylene terephthalates of component B are reaction products of aromatic dicarboxylic acids or their reactive derivatives, such as dimethyl esters or anhydrides, and aliphatic, cycloaliphatic or araliphatic
  • Preferred polyalkylene terephthalates contain at least 80% by weight, preferably at least 90% by weight, based on the dicarboxylic acid component of terephthalic acid residues and at least 80% by weight, preferably at least 90 mol%, based on the diol component of ethylene glycol and / or butanediol -l, 4-residues.
  • the preferred polyalkylene terephthalates can contain up to 20 mol%, preferably up to 10 mol%, of residues of other aromatic or cycloaliphatic dicarboxylic acids with 8 to 14 C atoms or aliphatic dicarboxylic acids with 4 to 12 C atoms, such as residues of phthalic acid, isophthalic acid, naphthalene-2,6-dicarboxylic acid, 4,4'-diphenyldicarboxylic acid, succinic acid, adipic acid, sebacic acid, azelaic acid, cyclohexanediacetic acid.
  • the preferred polyalkylene terephthalates can contain up to 20 mol%, preferably up to 10 mol%, other aliphatic diols with 3 to 12 C atoms or cycloaliphatic diols with 6 to 21 C -Atoms contain, e.g. B.
  • the polyalkylene terephthalates can be branched by incorporating relatively small amounts of trihydric or tetravalent alcohols or 3- or 4-basic carboxylic acids, for example according to DE-A 1 900 270 and US Pat. No. 3,692,744.
  • preferred branching agents are trimesic acid, trimellitic acid, trimethylol ethane and propane and pentaerythritol.
  • polyalkylene terephthalates which have been produced solely from terephthalic acid and its reactive derivatives (e.g. its dialkyl esters) and ethylene glycol and / or 1,4-butanediol, and mixtures of these polyalkylene terephthalates.
  • Preferred mixtures of polyalkylene terephthalates contain 0 to 50% by weight, preferably 0 to 30% by weight, polybutylene terephthalate and 50 to 100% by weight, preferably 70 to 100% by weight, polyethylene terephthalate.
  • Pure polyethylene terephthalate is particularly preferred.
  • Polyalkylene terephthalates with a high tendency to crystallize are particularly preferably used. These are characterized in that the isothermal crystallization time determined according to the method given in the example section is preferred
  • ⁇ 20 min particularly preferably ⁇ 10 min, in particular ⁇ 7 min.
  • the polyalkylene terephthalates preferably used generally have an intrinsic viscosity of 0.4 to 1.5 cm 3 / g, preferably 0.5 to 1.2 cm 3 / g, measured in phenol / o-dichlorobenzene (1: 1 parts by weight) at 25 ° C in the Ubbelohde
  • polyalkylene terephthalates can be prepared by known methods (for example, Kunststoff-Handbuch, volume VHI, p. 695 ff., Carl-Hanser-Verlag, Kunststoff 1973).
  • Component C can be prepared by known methods (for example, Kunststoff-Handbuch, volume VHI, p. 695 ff., Carl-Hanser-Verlag, Kunststoff 1973).
  • the composition according to the invention can preferably be one or more graft polymers of
  • the graft base C.2 generally has an average particle size (dso value) of 0.05 to 10 ⁇ m, preferably 0.1 to 5 ⁇ m, particularly preferably 0.1 to 1 ⁇ m, in particular 0.2 to 0.5 ⁇ m ,
  • Monomers C.I are preferably mixtures of
  • Methacrylonitrile and / or (meth) acrylic acid (C 1 -C 8 ) alkyl esters (such as
  • Methyl methacrylate, n-butyl acrylate, tert-butyl acrylate) and / or derivatives (such as anhydrides and imides) of unsaturated carboxylic acids for example
  • Preferred monomers C.1.1 are selected from at least one of the monomers styrene, ⁇ -methylstyrene and methyl methacrylate
  • preferred monomers C.1.2 are selected from at least one of the monomers acrylonitrile, maleic anhydride and methyl methacrylate.
  • Particularly preferred monomers are C.1.1 styrene and C.1.2 acrylonitrile.
  • Graft bases C.2 suitable for the graft polymers C are, for example, diene rubbers, EP (D) M rubbers, that is to say those based on ethylene propylene and, if appropriate, diene, acrylate, polyurethane, silicone, chloroprene and ethylene / vinyl acetate rubbers. Composites made from various of the rubbers mentioned are also suitable as a graft base.
  • Preferred graft bases C.2 are diene rubbers (for example based on butadiene, isoprene) or mixtures of diene rubbers or copolymers of diene rubbers or their mixtures with other copolymerizable monomers (for example according to C.1.1 and C.1.2), with the proviso that the glass transition temperature of Component C.2 is below ⁇ 10 ° C, preferably ⁇ 0 ° C, particularly preferably ⁇ -20 ° C, in particular ⁇ -40 ° C. Pure polybutadiene rubber is particularly preferred.
  • the gel fraction of the graft base B.2 is at least 30% by weight, preferably at least 40% by weight (measured in toluene).
  • the graft copolymers C are prepared by radical polymerization, for example by emulsion, suspension, solution or bulk polymerization, preferably by emulsion polymerization.
  • Particularly suitable graft rubbers are also ABS polymers that pass through
  • Redox initiation with an initiator system made of organic hydroperoxide and ascorbic acid according to US-A 4 937285.
  • the graft monomers are not necessarily grafted completely onto the graft base in the grafting reaction,
  • Graft polymers B are also understood to mean those products which are obtained by (co) polymerizing the graft monomers in the presence of the graft base and are also obtained in the working up.
  • Suitable acrylate rubbers according to C.2 of the polymers C are preferred
  • Acrylic acid alkyl esters optionally with up to 40% by weight, based on C.2, of other polymerizable, ethylenically unsaturated monomers.
  • the preferred polymerizable acrylic acid esters include C 1 to C 8 alkyl esters, for example methyl, ethyl, butyl, n-octyl and 2-ethylhexyl esters, and mixtures of these monomers.
  • Monomers with more than one polymerizable double bond can be copolymerized for crosslinking.
  • Preferred examples of crosslinking monomers are esters of unsaturated monocarboxylic acids with 3 to 8 C atoms and unsaturated monohydric alcohols with 3 to 12 C atoms, or saturated polyols with 2 to 4 OH
  • Groups and 2 to 20 carbon atoms such as ethylene glycol dimethacrylate, allyl methacrylate; polyunsaturated heterocyclic compounds such as trivinyl and triallyl cyanate; polyfunctional vinyl compounds such as di- and trivinylbenzenes; but also triallyl phosphate and diallyl phthalate.
  • Preferred crosslinking monomers are allyl methacrylate, ethylene glycol dimethacrylate, diallyl phthalate and heterocyclic compounds which have at least three ethylenically unsaturated groups.
  • crosslinking monomers are the cyclic monomers trialyll cyanurate, triallyl isocyanurate, triacryloylhexahydro-s-triazine and triallylbenzenes.
  • the amount of the crosslinked monomers is preferably 0.02 to 5, in particular 0.05 to 2,% by weight, based on the graft base C.2.
  • Preferred "other" polymerizable, ethylenically unsaturated monomers which, in addition to the acrylic acid esters, can optionally be used to prepare the graft base C.2 are, for. B. acrylonitrile, styrene, ⁇ -methylstyrene, acrylamides, vinyl d-C o -alkyl ether, methyl methacrylate, butadiene.
  • Preferred acrylate rubbers as the graft base C.2 are emulsion polymers which have a gel content of at least 60% by weight.
  • graft bases according to C.2 are silicone rubbers with graft-active sites, as are described in DE-A 3 704 657, DE-A 3 704 655, DE-A 3 631 540 and DE-A 3 631 539.
  • the gel content of the graft base C.2 is determined at 25 ° C. in a suitable solvent (M. Hoffmann, H. Krömer, R. Kuhn, Polymeranalytik I and II, Georg Thie e-Verlag, Stuttgart 1977).
  • the average particle size ds 0 is the diameter above and below which 50% by weight of the particles lie. It can be measured using an ultracentrifuge (W. Scholtan, H. Lange, Kolloid, Z. and Z. Polymer 250 (1972), 782-1796).
  • compositions according to the invention contain, as flame retardants, oligomeric phosphoric acid esters of the general formula (I)
  • R 1 , R 2 , R 3 and R 4 are preferably independently of one another C 1 -C 4 -alkyl, phenyl, naphthyl or phenyl-C-C 4 -alkyl.
  • the aromatic groups R 1 , R 2 , R 3 and R 4 can in turn be substituted by alkyl groups, preferably C. to C 4 alkyl.
  • Particularly preferred aryl radicals are cresyl, phenyl, xylenyl, propylphenyl or butylphenyl.
  • n in the formula (I), independently of one another, can be 0 or 1, preferably n is 1.
  • Compounds D of the structure are particularly preferred as component D.
  • the phosphorus compounds according to component D are known (see, for example, EP-A 0 363 608, EP-A 0 640 655) or can be prepared in an analogous manner by known methods (for example Ulimann's Encyclopedia of Industrial Chemistry, vol. 18, p. 301 ff. 1979; Houben-Weyl, Methods of Organic Chemistry, Vol. 12/1, p. 43; Beilstein Vol. 6, p. 177).
  • the mean q values can be determined by using a suitable method (gas chromatography (GC), high pressure liquid chromatography (HPLC), gel permeation chromatography (GPC)) to determine the composition of the phosphate mixture (molecular weight distribution) and from this the mean values for q be calculated.
  • a suitable method gas chromatography (GC), high pressure liquid chromatography (HPLC), gel permeation chromatography (GPC)
  • the flame retardants in accordance with component D are used in combination with so-called anti-dripping agents, which reduce the tendency of the material to burn in the event of a fire.
  • Compounds of the substance classes of fluorinated polyolefins, silicones and aramid fibers may be mentioned here as examples. These can also be used in the compositions according to the invention.
  • Fluorinated polyolefins are preferably used as anti-dripping agents. Fluorinated polyolefins are known and are described, for example, in EP-A 0 640 655. For example, they are marketed by DuPont under the Teflon® 30N brand.
  • the fluorinated polyolefins can be used both in pure form and in the form of a coagulated mixture of emulsions of the fluorinated polyolefins with emulsions of the graft polymers (component C) or with an emulsion of a copolymer, preferably based on styrene / acrylonitrile, the fluorinated polyolefin is mixed as an emulsion with an emulsion of the graft polymer or the copolymer and is then coagulated.
  • the fluorinated polyolefins can furthermore be used as a precompound with the graft polymer (component C) or a copolymer, preferably based on styrene / acrylonitrile.
  • the fluorinated polyolefins are mixed as a powder with a powder or granulate of the graft polymer or copolymer and are generally compounded in the melt at temperatures from 200 to 330 ° C. in conventional units such as internal kneaders, extruders or twin-screw screws.
  • the fluorinated polyolefins can also be used in the form of a masterbatch which is prepared by emulsion polymerization of at least one monoethylenically unsaturated monomer in the presence of an aqueous dispersion of the fluorinated polyolefin.
  • Preferred monomer components are styrene, acrylonitrile and mixtures thereof. After acidic precipitation and subsequent drying, the polymer is used as a free-flowing powder.
  • the coagulates, pre-compounds or masterbatches usually have fluorinated polyolefin contents of 5 to 95% by weight, preferably 7 to 60% by weight.
  • the quantity of fluorinated polyolefins relates to the absolute amount of fluorinated polyolefin.
  • compositions according to the invention can furthermore contain up to 10 parts by weight, preferably 0.1 to 5 parts by weight, of at least one conventional polymer additive, such as a lubricant and mold release agent, for example pentaerythritol tetrastate, a nucleating agent, an antistatic agent, a stabilizer Contain light stabilizers, a filler and reinforcing material, a dye or pigment and a further flame retardant or a flame retardant synergist, for example an inorganic substance in nanoscale form and / or a silicate material such as talc or wollastonite.
  • a lubricant and mold release agent for example pentaerythritol tetrastate
  • nucleating agent for example pentaerythritol tetrastate
  • an antistatic agent for example pentaerythritol tetrastate
  • a stabilizer Contain light stabilizers for example an antistatic agent
  • compositions according to the invention are prepared by mixing the respective constituents in a known manner and melt-compounding and melt-extruding them at temperatures from 200 ° C. to 300 ° C. in conventional units such as internal kneaders, extruders and twin-screw screws.
  • the individual constituents can be mixed in a known manner both successively and simultaneously, both at about 20 ° C. (room temperature) and at a higher temperature.
  • compositions according to the invention can be used for the production of moldings of any kind. These can be produced, for example, by injection molding, extrusion and blow molding. Another form of processing is the production of shaped bodies by deep drawing from previously produced sheets or foils.
  • moldings are foils, profiles, housing parts of any kind, e.g. For
  • Household appliances such as juicers, coffee machines, mixers; for office machines such as monitors, printers, copiers; plates, pipes, electrical installation ducts,
  • compositions according to the invention can be used, for example, to produce the following moldings or moldings:
  • Linear polycarbonate based on bisphenol A Makrolon® 2600, Bayer AG, Leverkusen (Germany)
  • Polyethylene terephthalate It is polyethylene terephthalate with an intrinsic viscosity IV of 0.74 cm 3 / g and an isothermal crystallization time
  • the intrinsic viscosity is measured in phenol / o-dichlorobenzene (1: 1 parts by weight) at 25 ° C.
  • the isothermal crystallization time of PET is determined with the DSC method (differential scanning calometry) with a PERKIN ELMER DSC 7 differential scanning calometer (weight approx. 10 mg, perforated aluminum pan) with the following temperature program:
  • the evaluation software is PE Thermal Analysis 4.00.
  • Component C is
  • Triphenyl phosphate Disflamol TP, Bayer AG, Leverkusen (Germany)
  • Resorcinol-bridged oligomeric phosphoric acid ester CR-733S, commercial product from Daihachi Chemical Industry Co., Ltd. (Japan)
  • Blendex® 449 Teflon masterbatch made from 50% by weight styrene-acrylonitrile copolymer and 50% by weight PTFE from GE Specialty Chemicals, Bergen op Zoom (Netherlands) FI component
  • PTS Pentaerythritol tetrastearate
  • the impact strength a ⁇ is determined in accordance with ISO 180 / 1A
  • the fire behavior is according to UL Subj. 94 V assessed on rods measuring 127 mm x 127 mm x 1.5 mm.
  • the heat resistance according to Vicat B is determined in accordance with ISO 306 on rods measuring 80 mm x 10 mm x 4 mm.
  • the elongation at break is determined in a tensile test according to ISO 527.
  • the impact strength at the weld line of test specimens molded on both sides and measuring 170 mm x 10 mm x 4 mm is measured.
  • the stress crack behavior (ESC behavior) is on bars of dimension
  • test specimens 80 mm x 10 mm x 4 mm examined. A mixture of 60 vol.% Toluene and 40 vol.% Isopropanol is used as the test medium.
  • the test specimens are pre-stretched using an arc template and stored in the above-mentioned test medium at room temperature. The stress crack behavior is assessed via the maximum pre-stretch (8 ⁇ ) at which no stress crack failure (ie no fracture) occurs in the test medium within 5 min. All test specimens were injection molded at an elevated processing temperature of 300 ° C.
  • the examples show that, surprisingly, the use of bisphenol A-bridged oligomeric phosphoric acid esters as flame retardant additives in PC / ABS / PET blends results in a significant improvement in the resistance to stress cracking at high processing temperatures, ie an extended processing window is realized.
  • the compositions show improved heat resistance with unchanged good impact strength, weld line strength, elongation at tear and flame resistance.
  • monophosphates here phenylphosphate
  • the stress cracking resistance drops significantly more with the processing temperature than with equivalent bisphenol diphosphate-based compositions.

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  • Compositions Of Macromolecular Compounds (AREA)

Abstract

L'invention concerne une composition contenant A) 40 à 95 parties en poids de polycarbonate aromatique et/ou de polyestercarbonate,B) 0,5 à 30 parties en poids de polyalkylèntérephthalate, C) 0,5 à 30 parties en poids de polymère greffé Pfropfpolymerisat, D) 0,5 à 25 parties en poids de composé phosphorique oligomère de la formule (I), (I) où R1, R2, R3, R4 représentent indépendamment les uns des autres alkyle C1-C8, cycloalkyle C5-C6, aryle C6-C10 ou aralkyle C7-C12, n vaut indépendamment 0 ou 1,q vaut 0,5 à 15, et E) 0 à 1 partie en poids de polyoéfine fluorée, la somme des parties en poids de ces composants étant égale à 100.
PCT/EP2003/007681 2002-07-29 2003-07-16 Matiere moulable ininflammable WO2004013227A1 (fr)

Priority Applications (6)

Application Number Priority Date Filing Date Title
JP2004525205A JP2005534755A (ja) 2002-07-29 2003-07-16 防炎成形組成物
MXPA05001112A MXPA05001112A (es) 2002-07-29 2003-07-16 Masas de moldeo resistentes a la llama.
CA002494349A CA2494349A1 (fr) 2002-07-29 2003-07-16 Matiere moulable ininflammable
BR0305682-1A BR0305682A (pt) 2002-07-29 2003-07-16 Massas para moldação ignìfugas
AU2003254360A AU2003254360A1 (en) 2002-07-29 2003-07-16 Flame-resistant moulding materials
EP03766177A EP1527136A1 (fr) 2002-07-29 2003-07-16 Matiere moulable ininflammable

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE10234419.1 2002-07-29
DE10234419A DE10234419A1 (de) 2002-07-29 2002-07-29 Flammwidrige Formmassen

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WO2004013227A1 true WO2004013227A1 (fr) 2004-02-12

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US (2) US20040039090A1 (fr)
EP (1) EP1527136A1 (fr)
JP (1) JP2005534755A (fr)
KR (1) KR20050029242A (fr)
CN (1) CN1701095A (fr)
AU (1) AU2003254360A1 (fr)
BR (1) BR0305682A (fr)
CA (1) CA2494349A1 (fr)
DE (1) DE10234419A1 (fr)
MX (1) MXPA05001112A (fr)
TW (1) TW200413468A (fr)
WO (1) WO2004013227A1 (fr)

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KR100831083B1 (ko) * 2005-12-27 2008-05-20 제일모직주식회사 고용융장력을 가지는 폴리에스테르계 열가소성 수지 조성물
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US8217101B2 (en) * 2007-03-02 2012-07-10 Bayer Materialscience Llc Flame retardant thermoplastic molding composition
WO2008138012A1 (fr) 2007-05-08 2008-11-13 3Form, Inc. Système de couleur à plusieurs variables avec application de texture
DE102009052042A1 (de) * 2009-11-05 2011-05-12 Bayer Materialscience Ag Polycarbonatzusammensetzung mit verbesserter Flammwidrigkeit für Extrusionsanwendungen
USD691289S1 (en) 2012-09-05 2013-10-08 3Form, Inc. Panel with cut and aligned thatch interlayer
CN103772934A (zh) * 2012-10-22 2014-05-07 黑龙江鑫达企业集团有限公司 一种高抗冲、高耐热pc/pbt合金材料及其制备工艺
CN105837859A (zh) * 2015-01-15 2016-08-10 张家港九力新材料科技有限公司 无机-有机磷酸酯共混复合阻燃材料的制备方法

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US7893135B2 (en) 2008-03-29 2011-02-22 Bayer Materialscience Ag Impact-modified polyalkylene terephthalate/polycarbonate compositions

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BR0305682A (pt) 2004-10-19
TW200413468A (en) 2004-08-01
EP1527136A1 (fr) 2005-05-04
JP2005534755A (ja) 2005-11-17
AU2003254360A1 (en) 2004-02-23
DE10234419A1 (de) 2004-02-12
US20060293422A1 (en) 2006-12-28
KR20050029242A (ko) 2005-03-24
MXPA05001112A (es) 2005-04-28
CA2494349A1 (fr) 2004-02-12
CN1701095A (zh) 2005-11-23
US20040039090A1 (en) 2004-02-26

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